تفاعل #1121794

ord-4a2695e74ca14d3bbbf8006355b6c42e

معادلة التفاعل

COC(CCC(=O)c1cc(Br)ccn1)OC
1-(4-bromo-pyridin-2-yl)-4,4-dimethoxy-butan-1-one
COC(CCC(=O)c1cc(Br)ccn1)OC
1-(4-Bromo-pyridin-2-yl)-4,4-dimethoxy-butan-1-one
O=C(O)C(F)(F)F
trifluoroacetic acid
O=CCCC(=O)c1cc(Br)ccn1
4-(4-bromo-pyridin-2-yl)-4-oxo-butyraldehyde
O=CCCC(=O)c1cc(Br)ccn1
4-(4-Bromo-pyridin-2-yl)-4-oxo-butyraldehyde

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe reaction is concentrated
  2. 2
    workup.DISSOLUTIONthe residue dissolved in ethyl acetate (150 mL)
  3. 3
    غسيلwashed with water 3 times
  4. 4
    تجفيفdried over Na2SO4
  5. 5
    أخرىthe solvent evaporated
  6. 6
    أخرىThe residue is purified by flash column chromatography (30% EtOAc in hexanes)

الإجراء التجريبي

To a solution of 1-(4-bromo-pyridin-2-yl)-4,4-dimethoxy-butan-1-one (2) (crude from Step 2, 11 g, 38.2 mmol) in 100 of CH2Cl2 at room temperature is added trifluoroacetic acid (10.9 g, 95.4 mmol) and the reaction mixture is stirred overnight. The reaction is concentrated, the residue dissolved in ethyl acetate (150 mL) and washed with water 3 times. The organic layers are combined, dried over Na2SO4 and the solvent evaporated. The residue is purified by flash column chromatography (30% EtOAc in hexanes) to give 4-(4-bromo-pyridin-2-yl)-4-oxo-butyraldehyde (3) as an yellow oil. (4.16 g, 45%): MS ES+244.04.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08546336B2uspto-grants-2013_10